Skip to main content
OpenTrials
Completed

NCT Number: NCT04663217

Exercise Hemodynamic, Right Ventricular Coupling and Echocardiography in Pulmonary Hypertension

This study aims to investigate the exercise profile in pulmonary hypertension patients with either pulmonary arterial hypertension, chronic thromboembolic pulmonary hypertension or pulmonary hypertension due to left heart disease and in disease control.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Kerckhoff-Klinik, Bad Nauheim, Hesse, Germany

Loading trial locations.

About this study

This is a dual-center observational prospective study in patients with pulmonary arterial hypertension, chronic thromboembolic pulmonary hypertension, pulmonary hypertension due to left heart disease. Patients undergoing right heart catheterisation due to dyspnoe with invasive exclusion of pulmonary hypertension will be recruited as disease control.

The study comprises a 1-day screening period, followed by a right heart catheterization with exercise challenge.

The study starts with screening, information of the patients and Informed Consent Form signature at day -1. Screening and inclusion of the patient can be performed on the same day. On the day of the planned right heart catheterization based on clinical grounds, exercise right heart catheterisation (RHC) using Swan-Ganz and/or Conductance catheters with simultaneous echocardiography will be performed. End of study is defined as a complete exercise RHC. Adverse events will be assessed until 1 day after the exercise RHC.

After placement of the Swan-ganz or Conductance catheter patients will undergo an exercise challenge using the following protocol in semi-supine position until exhaustion:

  • Incremental workload increase of 20Watt every 2-4 min.
  • For patients not able to start a 20 Watt, initial workload can be adjusted to a minimum of 5 Watt with 5 Watt increase every 2-4 min until exhaustion
  • Maximal exercise duration is 10-12 minutes
  • Symptoms of dyspnoea during exercise will be rated by subjects at baseline, after 6 minutes and at maximum according to the Borg perceived dyspnoea (0-10) scale.

Simultaneously, echocardiography and lung ultrasound will be performed before exercise (baseline), after 6 minutes of exercise and at maximum.

After assessment of right ventriclure pressure-volume loops during maximum exercise, guided by echocardiographic the conductance catheter will be placed in the right atrium to obtain right atrium pressure-volume loops during maximum exercise.

Optional, the exercise RHC will be performed without the Conductance catheter and only with the Swan-Ganz catheter. In this case, pressure values and cardiac output will be measured using the thermodilution method, averaging 3-5 measurements at baseline, 6 minutes and maximum. Detailed assessment of right atrial pressure curves (with a and v wave) will be performed at baseline, 6 minutes and maximum exercise.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed diagnosis of pulmonary arterial hypertension (World Health Organization group 1)
  • Pulmonary hypertension due to left heart disease (World Health Organization group 2)
  • Chronic thromboembolic pulmonary hypertension (World Health Organization group 4)
  • Invasive exclusion of pulmonary hypertension
  • Age ≥ 18 years
  • Planned right heart catheterization based on clinical grounds
  • Stable specific PAH medications
  • Ability to undergo cycle ergometry
  • Signed informed consent

Exclusion criteria

  • Other etiologic groups of pulmonary hypertension (World Health Organization group 3, 5)
  • Unstable or severe coronary artery disease
  • Uncontrolled arterial hypertension
  • Left ventricular ejection fraction < 30%
  • Severe congenital or acquired valvular or myocardial disease
  • Progressive left heart failure
  • History of severe ventricular arrhythmias
  • Severe, terminal renal impairment
  • Severe obstructive or restrictive lung disease
  • Severe lung emphysema or interstitial lung disease

Treatment and study plan

Exercise

Other

After placement of the right heart catheter patients will undergo an exercise challenge in semi-supine position until exhaustion

Primary outcomes

  1. exercise pulmonary arterial pressure

    Time frame: 1 day

    mean pulmonary arterial pressure (mmHg)

  2. exercise cardiac output

    Time frame: 1 day

    cardiac output (l/min);

  3. exercise pulmonary wedge pressure

    Time frame: 1 day

    pulmonary arterial wedge pressure (mmHg)

  4. exercise arterial elastance

    Time frame: 1 day

    arterial elastance (mmHg/mL)

  5. exercise end-systolic elastance

    Time frame: 1 day

    end-systolic elastance (mmHg/mL)

  6. exercise mean right atrial pressure

    Time frame: 1 day

    mean right atrial pressure (mmHg)

  7. exercise right atrial function

    Time frame: 1 day

    right atrial strain (%)

  8. exercise right volume

    Time frame: 1 day

    right ventricular volume (ml)

  9. exercise right ventriculare function

    Time frame: 1 day

    right ventricular strain (%)

  10. exercise right atrial volume-pressure curves

    Time frame: 1 day

    atrial volume to pressure ratio (ml/mmHg)

Secondary outcomes

  1. exercise lung congestion

    Time frame: 1 day

    B-Lines

  2. exercise left atrial function

    Time frame: 1 day

    left atrial strain (%)

  3. exercise left atrial volume

    Time frame: 1 day

    left atrial volume (ml)

  4. exercise hepatic backflow

    Time frame: 1 day

    diameter inferior vena cava (mm)

Sponsors and collaborators

Lead sponsor

University of Giessen

Other

Registry information

Acronym: EXERTION

Important dates

Study start
2020
Primary completion
2022
Study completion
2023
First posted
Dec 10, 2020
Registry last updated
May 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.